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腺嘌呤受体拮抗剂:三唑并三嗪和嘌呤支架可互换吗?

A Adenosine Receptor Antagonists: Are Triazolotriazine and Purine Scaffolds Interchangeable?

机构信息

Medicinal Chemistry Unit, School of Pharmacy, University of Camerino, Via Madonna delle Carceri, 62032 Camerino, Italy.

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze, 17/A, 43124 Parma, Italy.

出版信息

Molecules. 2022 Apr 7;27(8):2386. doi: 10.3390/molecules27082386.

Abstract

The A adenosine receptor (AAR) is one of the four subtypes activated by nucleoside adenosine, and the molecules able to selectively counteract its action are attractive tools for neurodegenerative disorders. In order to find novel AAR ligands, two series of compounds based on purine and triazolotriazine scaffolds were synthesized and tested at ARs. Compound was also tested in an in vitro model of neuroinflammation. Some compounds were found to possess high affinity for AAR, and it was observed that compound exerted anti-inflammatory properties in microglial cells. Molecular modeling studies results were in good agreement with the binding affinity data and underlined that triazolotriazine and purine scaffolds are interchangeable only when 5- and 2-positions of the triazolotriazine moiety (corresponding to the purine 2- and 8-positions) are substituted.

摘要

A 腺苷受体 (AAR) 是被核苷腺苷激活的四个亚型之一,能够选择性拮抗其作用的分子是神经退行性疾病的有吸引力的工具。为了寻找新型 AAR 配体,基于嘌呤和三唑并三嗪骨架的两个系列化合物被合成并在 ARs 上进行了测试。化合物 也在神经炎症的体外模型中进行了测试。一些化合物被发现对 AAR 具有高亲和力,并且观察到化合物 在小胶质细胞中表现出抗炎特性。分子建模研究结果与结合亲和力数据非常吻合,并强调三唑并三嗪和嘌呤骨架只有在三唑并三嗪部分的 5-和 2-位(对应于嘌呤的 2-和 8-位)被取代时才能互换。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93d8/9032385/bb1dcf4c7bc7/molecules-27-02386-g001.jpg

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